Azole type dioxolane derivatives
    7.
    发明授权
    Azole type dioxolane derivatives 失效
    唑型二氧戊环衍生物

    公开(公告)号:US4612322A

    公开(公告)日:1986-09-16

    申请号:US632852

    申请日:1984-07-20

    摘要: A compound of the formula: ##STR1## (wherein Az is imidazolyl or triazolyl;R is C.sub.1 -C.sub.5 alkyl or phenyl optionally substituted by 1 to 3 members selected from halogen, C.sub.1 -C.sub.5 alkyl, and C.sub.1 -C.sub.5 alkoxy;X.sup.1 and X.sup.2 each is hydrogen, halogen, C.sub.1 -C.sub.5 alkyl, or C.sub.1 -C.sub.5 alkoxy;Y is C.dbd.O, C.dbd.S, S.dbd.O, or R.sup.1 --C--R.sup.2 ; andR.sup.1 and R.sup.2 each is hydrogen, C.sub.1 -C.sub.3 alkyl or, taken together may form C.sub.4 -C.sub.6 alkylene)or its acid addition salt being useful as an antimycotic agent is prepared by reacting a corresponding diol with a cyclizing agent.

    摘要翻译: 下式的化合物(其中Az为咪唑基或三唑基; R为C1-C5烷基或任选被1至3个选自卤素,C 1 -C 5烷基和C 1 -C 5烷氧基的成员取代的苯基; X 1和X 2 各自为氢,卤素,C1-C5烷基或C1-C5烷氧基; Y为C = O,C = S,S = O或R1-C-R2; R1和R2各自为氢,C1-C3烷基 或一起可以形成C4-C6亚烷基)或其酸加成盐可用作抗真菌剂通过使相应的二醇与环化剂反应来制备。